Dextroamphetamine Sulfate Tablet
Product Images NDC 75826-121

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Dextroamphetamine Sulfate (NDC 75826-121). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Winder Laboratories Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Chemical Structure (Dextroamphetamine 01)

Chemical Structure (Dextroamphetamine 01)
Chemical structure of Dextroamphetamine Sulfate, depicting the molecular arrangement of the active ingredient including the sulfate component (H2SO4).*
FDA Label Image

Principal Display Panel (2.5 mg Tablet Bottle Label)

Principal Display Panel (2.5 mg Tablet Bottle Label)
Label for Dextroamphetamine Sulfate Tablets, USP 2.5 mg, containing 100 tablets per container. The label includes storage instructions (20° to 25°C), dispensing and usage notes, and the manufacturer Winder Laboratories LLC, Winder GA. The label also displays the NDC number 75826-120-10 and states 'Rx Only.'*
FDA Label Image

Principal Display Panel (10 mg Tablet Bottle Label)

Principal Display Panel (10 mg Tablet Bottle Label)
Label for Dextroamphetamine Sulfate Tablets USP 10 mg, oral tablets in a 100 count package from Winder Laboratories LLC, Winder GA. The label includes storage instructions at 20° to 25°C, directions for dispensing in a child-resistant container, and a note for pharmacists to provide the medication guide to patients. The NDC number 75826-123-10 is displayed.*
FDA Label Image

Principal Display Panel (15 mg Tablet Bottle Label)

Principal Display Panel (15 mg Tablet Bottle Label)
Label for Dextroamphetamine Sulfate Tablets, USP 15 mg, oral tablets, prescription only. The label includes the NDC 75826-124-10, package size of 100 tablets, and storage instructions at 20° to 25°C. It instructs pharmacists to dispense the medication guide to each patient and notes child-resistant packaging requirements. Labeler is Winder Laboratories LLC, Winder, GA.*
FDA Label Image

Principal Display Panel (20 mg Tablet Bottle Label)

Principal Display Panel (20 mg Tablet Bottle Label)
Label for Dextroamphetamine Sulfate Tablets, USP 20 mg by Winder Laboratories LLC. The label indicates 100 tablets per bottle with prescription-only status. Storage instructions suggest keeping the product at 20° to 25°C. It includes dispensing instructions and a note that pharmacists should provide medication guides. The NDC code is 75826-125-10.*
FDA Label Image

Principal Display Panel (30 mg Tablet Bottle Label)

Principal Display Panel (30 mg Tablet Bottle Label)
Label for Dextroamphetamine Sulfate Tablets USP 30 mg by Winder Laboratories LLC. The label indicates prescription use only, a quantity of 100 tablets, and storage instructions. It includes a barcode and space for lot/expiration details. The label emphasizes dispensing a medication guide with the product.*
FDA Label Image

Principal Display Panel (5 mg Tablet Bottle Label)

Principal Display Panel (5 mg Tablet Bottle Label)
Label for Dextroamphetamine Sulfate Tablets, USP 5 mg oral tablets by Winder Laboratories LLC. The label shows NDC 75826-121-10 and contains 100 tablets. It includes storage instructions, dispensing guidelines, and a barcode. The label states "Rx Only" and highlights the 5 mg strength.*
FDA Label Image

Principal Display Panel (7.5 mg Tablet Bottle Label)

Principal Display Panel (7.5 mg Tablet Bottle Label)
Label for Dextroamphetamine Sulfate Tablets, USP 7.5 mg, oral tablets in a 100-count package. The label includes storage instructions, pharmacist dispensing guidance, and a barcode. The product is manufactured by Winder Laboratories LLC, Winder GA, and is indicated as Rx only.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.